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Mirror movements (Version 1.0)

Level 2: Neurology and neurodevelopmental disorders

Panel types: Royal Melbourne Hospital, Rare Disease
Description
This panel contains genes that cause isolated congenital mirror movements. It does not contain genes associated with mirror movements as a component of a syndromic phenotype.
Panel Activity

1 reviewer

  • Bryony Thompson (Royal Melbourne Hospital)

4 Entities

4 reviewed, 3 green

List Entity Reviews Mode of inheritance Details
4 Entitiess
Green List (high evidence)
DCC
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600
Tags
Green List (high evidence)
NTN1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Mirror movements 4 MIM#618264
Tags
Green List (high evidence)
RAD51
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Mirror movements 2 MIM#614508
Tags
Red List (low evidence)
DNAL4
1 review
1 red
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
Phenotypes
  • Mirror movements 3 MIM#616059
Tags

Major version comments

  • 2021-09-02 02:08 Bryony Thompson (Royal Melbourne Hospital) promoted panel to 1.0
    All genes on panel reviewed, ready for promotion.

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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